Upload your 23andMe file. In minutes, get personalized supplement stacks, drug interaction warnings, disease risk analysis, and a 90-day action plan backed by 341,000+ clinically-reviewed variants.
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23andMe tells you where your ancestors are from. We tell you which supplements to take, which drugs to avoid, and what diseases to screen for.
Each report is generated from your raw DNA data, cross-referenced against the world's largest clinical databases.
How your body processes drugs, nutrients, and supplements. Covers CYP enzymes, MTHFR methylation, COMT, caffeine metabolism, vitamin absorption, muscle fiber type, and sleep genetics.
Scans your genome against 341,000+ ClinVar variants to identify pathogenic mutations, carrier status for recessive conditions, drug response variants, and protective alleles.
A personalized daily protocol built from your genetics: morning/midday/evening supplement stacks, dietary targets, exercise framework, monitoring schedule, and a 90-day checklist.
We cross-reference your DNA against ClinVar (NIH's clinical variant database with 341K+ entries) and PharmGKB (Stanford's pharmacogenomics database). These are the same sources your doctor would use.
Other services hand you a spreadsheet of SNPs and say "good luck." We give you exact supplement names, dosages, timing (morning/evening), dietary macros, and a week-by-week implementation plan.
Our AI chat has full context of your genetic results. Ask it anything: "Should I take methylfolate?", "Am I a poor metabolizer of caffeine?", "What does my MTHFR status mean for pregnancy?"
Your genome data is encrypted, processed on isolated servers, and deletable at any time from your settings. We never sell or share your genetic data. Period.
If you're a poor metabolizer of certain enzymes, common medications can be dangerous. We flag every drug-gene interaction from PharmGKB's clinical annotation database so you know before your doctor prescribes.
Discover if you carry recessive variants for conditions like cystic fibrosis, sickle cell, or hereditary hemochromatosis. Critical information if you're planning to have children.
Log into 23andMe, go to Settings, and download your raw data file. It's a text file you already own.
Create your free account and drag-and-drop your file. Processing takes under 10 minutes.
Receive three detailed reports and start your personalized 90-day health protocol immediately.
"I've had my 23andMe data for 3 years and never knew I was a poor CYP2D6 metabolizer. My doctor had me on codeine for pain, and it literally doesn't work for me. This report may have saved my life."
Michael R.
Software Engineer
"The methylation report alone was worth it. I found out I have compound heterozygous MTHFR, which explains years of fatigue and brain fog. The supplement protocol with methylfolate changed everything within weeks."
Sarah L.
Nurse Practitioner
"My wife and I both ran our DNA before starting a family. Discovered we're both carriers for the same recessive condition. Our genetic counselor confirmed it. Information we never would have found on our own."
James K.
Product Manager
| Feature | 23andMe | Promethease | Your DNA Unlocked |
|---|---|---|---|
| Personalized supplement stacks | |||
| Drug interaction warnings | Basic | Raw data | |
| ClinVar disease analysis (341K+) | |||
| Diet & exercise protocol | |||
| AI chat about your results | |||
| 90-day implementation plan |
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